Trobaugh-Lotrario et al 1 are to be congratulated on their detailed review of cases of
Beckwith-Wiedemann Syndrome (BWS) with hepatoblastoma. We think that details …

Following the discovery of a fetal hepatic tumor, labor was induced at 38 weeks, and a
phenotypically normal female was delivered vaginally. A serum alpha-fetoprotein level at …

Patients with Beckwith–Wiedemann syndrome (BWS) have an increased risk to develop
cancer in childhood, especially Wilms tumor and hepatoblastoma. The risk varies depending …

Abstract The Beckwith-Wiedemann syndrome is a cancer predisposition syndrome
characterized by a predilection to embryonal tumor growth, especially Wilms tumor …

Beckwith–Wiedemann syndrome (BWS) is a rare overgrowth syndrome associated with an
increased risk in childhood tumours. The phenotypic variability in BWS reflects its molecular …

Abstract Patients with Beckwith-Wiedemann Syndrome (BWS) are predisposed to
developing hepatoblastoma. Clinical data were reviewed in all cases of hepatoblastoma in …

Objective To compare tumor risk in the 4 Beckwith-Wiedemann syndrome (BWS) molecular
subgroups: Imprinting Control Region 1 Gain of Methylation (ICR1-GoM), Imprinting Control …

Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth disorder mainly
associated with altered genomic imprinting at chromosome 11p15. 5. Children with BWS …

Simple Summary Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn
overgrowth disorder caused by molecular alterations in chromosome 11p15. 5. These …

Beckwith–Wiedemann syndrome is an overgrowth disorder characterized by neonatal
macrosomia, abdominal wall defects, macroglossia, renal anomalies, organomegaly …